Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Soluble polythiophene derivatives

a technology of soluble polythiophene and derivatives, which is applied in the direction of organic dyes, azo dyes, chemistry apparatuses and processes, etc., can solve the problems of limiting the practicability of optoelectronic devices made of polymer semiconducting materials, reducing the power conversion efficiency of oscs, etc., and achieves the degree of intramolecular conjugation and intermolecular - interaction, increasing carrier mobility, and improving the degree of intramolecular

Inactive Publication Date: 2010-07-13
IND TECH RES INST
View PDF1 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides a new type of soluble polythiophene derivative with highly coplanar repeating units. This structure improves the degree of intramolecular conjugation and intermolecular π-π interaction, which increases carrier mobility. The new compound has the formula (I) or (II) and can be used in various applications such as electronics, sensors, and optics.

Problems solved by technology

However, a main drawback for conjugated polymer applicability in optoelectronic devices is its low carrier mobility, consequently limiting the practicability of optoelectronic devices made with polymer semiconducting material.
Otherwise, if the electrons and holes recombine, the carrier function will disappear, thus reducing power conversion efficiency of the OSCs.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Soluble polythiophene derivatives
  • Soluble polythiophene derivatives
  • Soluble polythiophene derivatives

Examples

Experimental program
Comparison scheme
Effect test

example 1

Preparative Example 1

Synthesis of p-thiophene-phenylene-thiophene (S2)

[0044]

[0045]Scheme 1 depicts the synthesis of compound S2. Compound 8 was prepared by the synthetic method described in Org. Lett. 2006, 8, 5033-5036. 626 mg (1 mmol) of Compound 8 and 392 mg (2.2 mmol) of N-Bromosuccinimide (NBS) were dissolved in 20 mL of chloroform in a 100 mL two-necked bottle. The bottle was wrapped by Al foil and kept under N2 atomsphere overnight. The organic phase was extracted by a chloroform and saturated sodium chloride solution. Next, the organic phase was dried over anhydrous MgSO4 and filtered. The filtrate was concentrated on a rotary evaporator. A pale yellow solid S2 was obtained after precipitation by methanol.

[0046]NMR data of the compound S2 was as follows.

[0047]1H NMR (CDCl3, 200 MHz) δ 2.29 (s, 12H), 6.94 (s, 2H), 7.05˜7.12 (m, 16H), 7.29 (s, 2H).

Preparative Example 2

Synthesis of m-thiophene-phenylene-thiophene (S3)

[0048]

[0049]Scheme 2 depicts the synthesis of compound S3. Co...

example

Example 1

Synthesis of Polymer P6

[0069]

[0070]Scheme 7 depicts the synthesis of compound P6. 0.3 mmol of p-TPT, 5.5 mg (2 mol %) of 5,5′-Bis-trimethylstanny 4,4′-bis(decyl)-2,2′-bithiophene, 14.6 mg (16 mol %) of tri(o-tolyl)phosphine and 5 mL of chlorobenzene were placed in a glass flask. After deoxygenation, the flask was placed in a microwave reactor (640 W, 30 min) for polymerization. After cooled to room temperature, the reaction mixture was added to methanol for precipitation. The polymer was filtered out and cleaned by using MeOH, acetone and hexane soxhelt extraction and chloroform was used to dissolve the polymer. Removal of the chloroform resulted in the polymer P6 (molecular weight: 25200 g / mol, λmax=490 (film)).

example 2

Synthesis of Polymer P8

[0071]

[0072]Scheme 8 depicts the synthesis of compound P8. 0.3 mmol of p-TPT, 5.5 mg (2 mol %) of 5,5′-Bis-trimethylstanny 4,4′-bis(decyl)-2,2′-bithiophene, 14.6 mg (16 mol %) of tri(o-tolyl)phosphine and 5 mL of chlorobenzene were placed in a glass flask. After deoxygenation, the flask was placed in a microwave reactor (640 W, 30 min) for polymerization. After cooled to room temperature, the reaction mixture was added to methanol for precipitation. The polymer was cleaned by using MeOH, acetone and hexane soxhelt extraction and chloroform was used to dissolve the polymer. Removal of the chloroform resulted in the polymer P8 (molecular weight: 16900 g / mol, λmax=442 (film)).

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
channel lengthaaaaaaaaaa
channel lengthaaaaaaaaaa
open-circuit voltageaaaaaaaaaa
Login to View More

Abstract

The present invention discloses a soluble polythiophene derivative containing highly coplanar repeating units. The coplanar characteristic of the TPT (thiophene-phenylene-thiophene) units improves the degree of intramolecular conjugation and intermolecular π-π interaction. The polythiophene derivative exhibits good carrier mobility and is suitable for use in optoelectronic devices such as organic thin film transistors (OTFTs), organic light-emitting diodes (OLEDs), and organic solar cells (OSCs).

Description

BACKGROUND OF THE INVENTION[0001]1. Field of the Invention[0002]The present invention relates to a soluble polythiophene derivative containing highly coplanar repeating units, and in particular relates to using the soluble thiophene derivative in optoelectronic devices.[0003]2. Description of the Related Art[0004]Recently, due to the fundamental semiconductor and optoelectronic properties of polymer semiconducting material, the material has attracted considerable research interest because of the potential for being used in optoelectronic devices such as organic thin film transistors (OTFTs), organic light-emitting diodes (OLEDs), and organic solar cells (OSCs) and being mass produced. In addition, with the active layer of the optoelectronic device being fabricated by printing technology, material having polymer properties can produce a flexible optoelectronic device with advantages of light-weight, low cost and large area fabrication.[0005]The key development for polymer semiconduct...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(United States)
IPC IPC(8): C08G75/00
CPCC08F128/06C09B69/109C09B57/00
Inventor CHAN, SHU-HUACHAO, TENG-CHIHKO, BAO-TSANCHEN, CHIH-PINGLIN, CHIN-SHENGCHEN, YI-LING
Owner IND TECH RES INST
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com